EP2052183B1 - Système de chauffage activé par l'oxygène et méthodes de réalisation dudit système - Google Patents

Système de chauffage activé par l'oxygène et méthodes de réalisation dudit système Download PDF

Info

Publication number
EP2052183B1
EP2052183B1 EP07800084.1A EP07800084A EP2052183B1 EP 2052183 B1 EP2052183 B1 EP 2052183B1 EP 07800084 A EP07800084 A EP 07800084A EP 2052183 B1 EP2052183 B1 EP 2052183B1
Authority
EP
European Patent Office
Prior art keywords
substrate
heating apparatus
stock
portable flameless
oxygen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP07800084.1A
Other languages
German (de)
English (en)
Other versions
EP2052183A4 (fr
EP2052183A2 (fr
Inventor
Lawrence A. Tinker
Ramesh C. Kainthla
Charles Edward Sesock
Bhavesh Patel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rechargeable Battery Corp
Original Assignee
Rechargeable Battery Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rechargeable Battery Corp filed Critical Rechargeable Battery Corp
Publication of EP2052183A2 publication Critical patent/EP2052183A2/fr
Publication of EP2052183A4 publication Critical patent/EP2052183A4/fr
Application granted granted Critical
Publication of EP2052183B1 publication Critical patent/EP2052183B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/16Materials undergoing chemical reactions when used
    • C09K5/18Non-reversible chemical reactions
    • AHUMAN NECESSITIES
    • A47FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47JKITCHEN EQUIPMENT; COFFEE MILLS; SPICE MILLS; APPARATUS FOR MAKING BEVERAGES
    • A47J36/00Parts, details or accessories of cooking-vessels
    • A47J36/24Warming devices
    • A47J36/30Devices for warming by making use of burning cartridges or other chemical substances
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24HEATING; RANGES; VENTILATING
    • F24VCOLLECTION, PRODUCTION OR USE OF HEAT NOT OTHERWISE PROVIDED FOR
    • F24V30/00Apparatus or devices using heat produced by exothermal chemical reactions other than combustion

Definitions

  • the present invention relates to portable flameless heaters that produce heat upon reaction with oxygen and methods of manufacturing and packaging same.
  • Portable flameless heaters are currently used in a variety of applications, for example heating comestible items.
  • FRH flameless ration heater
  • MRE mean ready to eat
  • MRE mean ready to eat
  • 8-ounce approximately 227 grams
  • the FRH consists of a super-corroding magnesium/iron mixture sealed in a waterproof pouch (total FRH weight is approximately 22 grams).
  • the pouch is opened into which the MRE is inserted, and approximately 58 grams of water is added to a fuel-containing portion of the FRH pouch surrounding the MRE to initiate the following reaction: Mg + 2H 2 O ⁇ Mg(OH) 2 + H 2
  • the MRE temperature is raised by approximately 37.8°C (100°F) in less than 10 minutes.
  • the maximum temperature of the system is safely regulated to about 100°C (212°F) by evaporation and condensation of water vapor.
  • the current FRH while effective for its intended purpose, produces hydrogen gas as a byproduct generating safety, transportation, storage and disposal concerns, and making it less suitable for use in consumer sector applications where accidental misuse could lead to fire or explosion.
  • the water required for reaction in addition to being heavy and spacious, is typically obtained from a soldier's drinking water supply, which is often limited. Addition of the water can also be an inconvenient additional step in the process of activating the FRH.
  • Self-heating food packaging products are also available in the consumer market. These products use the heat of hydration from mixing "quicklime” (calcium oxide) and water (CaO + H 2 O ⁇ Ca(OH) 2 ) which does not generate hydrogen. With water present the peak temperature is similarly limited to 100°C (212°F) but even neglecting the weight of packaging and water, the specific energy of the system is low (approximately 1.2 kJ per gram of CaO). These and other self-contained systems must also provide some means of mixing the segregated reactants adding further complexity and bulk. Measurements on some commercial self-heating packaged food products are shown in Table 1.
  • Table 1 Food product (net) Total package (gross) Specific energy of heater (kJ/g) Weight (g) Volume (ml) Weight (g) Volume (ml) Coffee 300 295 551 600 0.34 Beef stew 425 481 883 963 0.13
  • quicklime based heaters may offer greater safety than the Mg based heaters
  • quicklime heaters significantly lower specific energy and cause the weight and size of the heater to approach that of the object being heated, reducing portability.
  • Oxygen-based heaters such as those described in U.S. Pat. Nos. 5,984,995 , 5,918,590 and 4,205,957 , have certain benefits over water-based heaters.
  • oxygen-based heaters do not require the addition of water to generate heat.
  • the reaction may be stopped by preventing oxygen access and restarted at a later time.
  • EP 1 439 213 A1 discloses a composition containing a heat-generating substance generating heat upon reaction with oxygen, a carbon component, an oxidation promoter and water as well as a water separation-preventing stabilizer. This composition may be molded on base material etc.
  • US 4,268,272 A discloses an exothermic composition comprising a fibrous powder.
  • US 5,180,759 A and EP 0 244 133 A2 disclose an exothermic composition
  • a particulate readily oxidisable metal and an organic fluorine-containing compound which may be polytretrafluoroethylene, optionally filled with carbon.
  • the exothermic composition When used in the form of a preformed shape, it also contains one or more binders different from tetrafluoropolyethylene.
  • US 6,209,457 B1 discloses an exothermic composition material for controlled localized heating of a base material comprising an exothermic self-propagating high-temperature synthesis gasless combustion material mixture having a predetermined temperature of burning which may be selected from combinations of certain metals with carbon. Theses certain metals are Ti, Hf, Nb, Ta, and Zr.
  • the invention relates to a precursor of a portable flameless heating apparatus, that can be comprised in a portable flameless heating apparatus, as defined in claim 1, the portable flameless heating apparatus comprising a flexible porous substrate formed into a desired shape, the substrate includes a reducing agent providing an exothermic reaction upon oxidation, a promoter for the reduction of oxygen, and a binding agent.
  • a portable flameless heating apparatus as defined in claim 2 which will generate heat upon reaction with oxygen once electrolyte is added. Unlike the water-based heaters, the present heater takes advantage of the ambient oxygen present in the atmosphere.
  • Yet another aspect of the invention relates to a method of manufacturing a portable flameless heating apparatus as defined in claim 9 generally comprises the steps of mixing a reducing agent, a promoter for reducing oxygen, and a binding agent to form a mixture.
  • the mixture is then formed into a substrate with a desired shape, and, then stored in ambient or another oxygen- containing atmosphere.
  • This aspect has substantial benefits in the manufacturing process.
  • the method allows a substrate to be produced and stored for a commercially acceptable period of time until the substrate is needed to produce a specific portable flameless heating apparatus configuration.
  • the desired shape of the substrate may initially be a stock shape sized for later reforming or dividing into smaller sizes as desired for use with differing applications. This too is believed to have substantial benefits for a manufacturing process such as, allowing multiple heater designs to be made from one stock material.
  • Other benefits of this aspect of the invention will be appreciated and understood based upon the description of the preferred embodiments.
  • a portable flameless heating apparatus comprises a flexible porous substrate formed into a desired shape, the substrate includes a reducing agent providing an exothermic reaction upon oxidation, a promoter for the reduction of oxygen, and a binding agent.
  • the reducing agent is preferably selected from the group consisting essentially of: zinc, aluminum, or magnesium.
  • the promoter is carbon and may or may not have addition chemicals or compositions added to it.
  • the substrate includes an electrolyte.
  • the electrolyte is alkaline, preferably potassium hydroxide.
  • the binding agent is preferably chosen to assist in providing porosity in the substrate and according to one aspect of the invention to also aid in allowing the substrate to be flexible.
  • the binding agent is polytetrafluoroethylene which aids in providing both of these attributes.
  • the polytetrafluoroethylene may be in the range of 1% to 40% of the total weight of the substrate.
  • the binding agent may comprise a mixture of chemical compounds.
  • a substrate with an integral shape as opposed to simply providing a particulate mixture of the chemical constituents of the heater, provides the benefits accompanying the use of integral structures in product design, for example, structural integrity of the heater.
  • the flexibility of the portable flameless heating apparatus supplies numerous benefits. For example, as a preformed stock material or packaged heater, a portable flameless heating apparatus may be bent, or displaced, to fit containers having varied shapes and dimensions.
  • the portable flameless heating apparatus When charged with an electrolyte, the portable flameless heating apparatus further comprises a container surrounding the porous substrate to segregate the substrate from an atmosphere outside of the container.
  • the container has at least one re-sealable opening to selectively permit ambient atmosphere to access the substrate for purposes of oxygen reaction with the substrate.
  • a re-sealable opening may include (but certainly is not limited to): pressure sensitive adhesive, mechanical tongue-and-grove structure, elastic or twist locks, or any other structure that may selectively permit resealing the opening.
  • the opening includes an oxygen-permeable barrier to cover the substrate when the opening is unsealed to maintain physical isolation or sequestration of the substrate within the container while permitting access to oxygen.
  • Varying the permeability of the barrier may be used to control the rate of heat production.
  • a barrier that allows a large flow of oxygen in will allow for a faster rate of reaction, and a barrier that lets a small amount of oxygen in will allow for a slower rate of reaction.
  • FIG. 1 discloses a portable flameless heating apparatus 5.
  • the portable flameless heating apparatus 5 comprises a substrate 6 (in the form of a thick, or plate-like sheet) is surrounded (for segregation from the atmosphere) by a container 7 which has front flap 8 and a back flap 9 both of which are oxygen-impermeable (it is recognized that materials which have a relatively low level of oxygen-permeability may be used).
  • the front flap 8 has a pressure sensitive adhesive 10 around a marginal edge perimeter thereof.
  • the front flap 8 (when closed) segregates the substrate 6 from oxygen.
  • the front flap 8 may be partially removed to expose an opening 11, which in turn exposes the substrate 6 to oxygen.
  • Within the opening 11 there is an oxygen-permeable barrier 12.
  • the oxygen-permeable barrier 12 secures the substrate 6 in the container 7.
  • the oxygen-permeable barrier 12 has apertures 14 which allow oxygen to reach the substrate 6 of the portable flameless heating apparatus 5. Once the item to be heated has been heated to the desired temperature, the front flap 8 may be used to close the opening 11 and the pressure sensitive adhesive portion 10 may hold the front flap 8 in place while providing an air-occlusive seal. The reaction will stop producing heat once all of the oxygen within the container 7 has been reacted.
  • the reaction is oxygen based, the reaction can be stopped by closing the opening(s) and cutting off oxygen access. If not all of the reducing agent has reacted, the portable flameless heating apparatus, unlike water based heaters, may be restarted and used to subsequently heat the same or a second item.
  • the portable flameless heating apparatus comprises a flexible porous substrate formed into a desired shape, the substrate including a reducing agent selected from the group consisting essentially of: zinc, aluminum, or magnesium providing an exothermic reaction upon oxidation, carbon as promoter for the reduction of oxygen, an alkaline electrolyte, and, a polytetrafluoroethylene binding agent, and, a container surrounding the substrate to segregate the substrate from an atmosphere outside of the container, the container having at least one re-sealable opening to selectively permit ambient atmosphere to access the substrate for purposes of oxygen reaction with the substrate.
  • a reducing agent selected from the group consisting essentially of: zinc, aluminum, or magnesium providing an exothermic reaction upon oxidation, carbon as promoter for the reduction of oxygen, an alkaline electrolyte, and, a polytetrafluoroethylene binding agent
  • the desired shape of a substrate may be formed to have a preformed contour substantially mating with a contour of a portion of the outer surface of a container (such as a container for containing a substance to be heated such as a comestible) required for the desired heat transfer from the apparatus to the contents of the container.
  • a container such as a container for containing a substance to be heated such as a comestible
  • the substrate for example, may be molded, pressed into a mold or is wrapped around the outer surface of the container.
  • FIG. 2 discloses a portable flameless heating apparatus 20 which is preformed into a desired shape 22.
  • the desired shape 22 mates with the contour 24 of a portion 26 of the outer surface 28 of a container 30 which may contain a comestible.
  • Another desired shape of a substrate is a stock shape sized for later reforming or dividing into smaller sizes as desired for use with differing applications. It is believed that any suitable method may be used to manufacture the stock shape, including, but not limited to, rolling, extruding, pressing, forming, stretching, etc.
  • the stock shape may be any shape, including, but not limited to, conventional sheet stock, rod stock, bar stock, and tube stock.
  • Sheet stock may be a thick sheet, e.g. "plate,” or it may be a thin sheet, e.g., "film.”
  • Rod stock too, may be a thick rod, or a thin rod, like a rope or a wire.
  • bar stock and tube stock may be thick or thin, depending on the desired application.
  • the stock material may be extruded cylinders, triangles, square tubes or any other shape. The stock material is sized for later reforming or dividing into smaller sizes for use or further reforming as desired for use with differing applications.
  • thinner desired shapes and thinner stock shapes Utilizing thinner desired shapes and thinner stock shapes is believed to have additional benefits. For example, a thinner sheet may be wrapped around a container multiple times instead of using a single wrap with a thick stock. Similarly, a thinner rod or "wire" may also be wrapped around a container, e.g ., wound. The thinner shapes are believed to have increased flexibility. Additionally, by utilizing thinner shapes, it is contemplated that the portable flameless heating apparatus may not need adhesive or other structure or composition to assist in keeping it disposed adjacent to the container or object to be heated.
  • Another aspect of the invention provides a novel method to construct a portable flameless heating apparatus.
  • FIG. 3 discloses a preferred method 31 according to this aspect of the invention.
  • the method comprises the steps of mixing (32) a reducing agent, a promoter for reducing oxygen, and a binding agent to form a mixture, forming (33) the mixture into a substrate with a desired shape, and, then storing (34) the substrate in ambient or other oxygen containing atmosphere.
  • storing it is meant that the substrate can be stored for a commercially acceptable period, or "shelf life," such that based upon the concentration, the porosity of the substrate, the chemicals comprising the substrate, and other factors, the substrate will still be able to produce the required heat when the substrate is integrated into an end use such as a heater.
  • the desired shape is flexible.
  • step (33) the desired shape of the substrate may be preformed into a contour substantially mating with a contour of a portion of an outer surface of a container for containing a comestible required for the desired heat transfer from the apparatus to the comestible e.g. see FIG. 2 .
  • the desired shape of the substrate may be formed as a stock shape, as described above, which may include the later step (35) of reforming or dividing the stock material into smaller sizes substrates as desired for use with differing applications.
  • the stock shape may be any shape, including, but not limited to, sheet stock, rod stock, bar stock, and tube stock.
  • Sheet stock may be a thick sheet, e.g. "plate,” or it may be a thin sheet, e.g., "film.”
  • Rod stock, too, may be a thick rod, or a thin rod, like a wire.
  • bar stock and tube stock may be thick or thin, depending on the desired application.
  • the stock material may be extruded cylinders, triangles, square tubes or any other shape.
  • the stock material is sized for later reforming or dividing into smaller sizes for use or further reforming as desired for use with differing applications. As noted above it is believed that the thinner desired shapes and thinner stock shapes may have additional benefits from thicker stock in terms of manufacturing and design flexibility and scalability.
  • the inventors of the present invention have determined that varying the concentration of the electrolytic solution can control the rate of the reaction. For example, if a desired application needs a faster more immediate need of heat (higher temperature or flux), as may be required for suitably heating a container of food in an acceptable time frame, then an electrolyte with a relatively higher concentration may be used. However, if a longer, more prolonged heat generation or lower temperature is required for the substance to be heated, then an electrolyte with a lower concentration may be used. Utilizing this aspect in the manufacturing process can have substantial benefits for scalability and reduced part count, as is true for the other aspects of the invention disclosed herein i.e. flexibility of the substrate, manufacturing stock shapes of the substrate, and manufacturing and storage of the substrate in ambient air.
  • selecting the concentration of the electrolyte after substrate manufacture allows a manufacturer to mass-produce a stock material, which may be produced in an ambient atmosphere wherein oxygen is present, then, as the need arises, the stock material may be reformed or divided and then reformed into smaller portable substrates for various applications before the electrolyte is added.
  • the electrolyte may then be selected and matched with substrates for further packaging for various differing applications.
  • a method of manufacturing a portable flameless heating apparatus may further comprise the step (36) of selecting a desired rate of reaction as influenced by the electrolyte, and/or selecting an electrolytic solution to provide the selected rate of reaction, and, then provide the step (37) of adding the selected electrolytic solution to the substrate.
  • the rate of reaction is controlled, at least in part by utilizing an appropriate electrolyte concentration.
  • the electrolyte since the reaction is driven by oxygen, and will only begin once the electrolyte is added, the electrolyte may be added in an oxygen containing atmosphere. This may have additional benefits in the manufacturing process. For example, there would be no need to create an oxygen-free atmosphere for the manufacturing process.
  • Sequestering or encasing the portable substrate such as in packaging may be conducted in such a way as to permit only a negligible amount of reaction, such as by varying packaging time, amount of reagent used, etc. Once contained, the reaction will create a negative pressure (within the container), which advantageously will aid in initially drawing oxygen in as the heater is later put into use and exposed to oxygen by a user.
  • a method of manufacturing may further comprise the step (38) of segregating, such as by surrounding the substrate in a container to segregate the substrate from an atmosphere outside of the container, wherein the container has at least one re-sealable opening to selectively permit ambient atmosphere to access the substrate for purposes of oxygen reaction with the substrate.
  • the ball was formed into a rectangular shaped brick.
  • the rectangular shape was then processed through a roll milling process to form thinner and thinner sheets stopping at a final desired thickness for the particular type of heater sheet.
  • the sheet was then placed in an oven at 95 °C to dry. After removing the sheet from the oven the resulting heater sheet is porous, cohesive and flexible, and may be cut into any desired dimensions for the particular application.
  • the dry non-activated heater sheets can be stored in normal atmospheric conditions indefinitely, for use later as a heater.
  • Other suitable methods of constructing the heater may include similar methods of extruding, roll coating, casting, or pasting known to those of skill in the art.
  • a portable flameless heating apparatus prepared as described above, was taken into an inert atmosphere glove box. The material was then wetted with a 9N KOH solution (approximately 37% by weight). Approximately 23% by weight of KOH was added to the portable flameless heating apparatus. After the solution had soaked into the pores of the sheet, the sheet was formed to the outside circumference of a metal soup can. This can was then placed inside a larger can with an outer wall that provided openings. This can assembly was then placed in a sealed oxygen impermeable membrane to prevent it from being exposed to oxygen. The assembly was then removed from the glove box. The assembly was removed from the plastic bag and approximately 290 milliliters of water to be heated was added to the inner soup can. Two thermocouples were placed inside the soup can and a lid placed over the can. An additional thermocouple was placed on the surface of the sheet heater material.
  • FIG. 4 discloses that the portable flameless heating apparatus began to generate heat immediately after being exposed to the air.
  • the maximum temperature reached on the heater surface 40 was approximately 126.7 °C (260 °F).
  • the water temperature 42, 44 inside the soup can was raised to 88.3 °C (191 °F) from a starting temperature of 21.2 °C (70 °F).
  • FIG. 5 discloses a second sample, wherein the heater surface 50 temperature was measured and the water temperature 52, 54 was raised to 93.3 °C (201 °F).
  • a third example of a portable flameless heating apparatus was prepared as described above and utilized to heat water in a flexible pouch similar to an MRE pouch.
  • the portable flameless heating apparatus was placed on the outside surfaces of the pouch and sealed from the air. Inside the pouch on each side, directly opposite the portable flameless heating apparatus was an absorbent material that was wetted with water. The pouch was removed from the inert atmosphere.
  • a water filled MRE pouch was placed inside the heater pouch. The water filled pouch was monitored with a thermocouple to determine the temperature change of the water over time.
  • the portable flameless heating apparatus was then exposed to the air by removing the seals and allowing oxygen in the surrounding air, access to the heater.
  • the portable flameless heating apparatus began to heat up and generated enough heat to raise the water temperature to 76.7 °C (170 °F) within approximately 9 minutes.
  • FIG. 6 discloses a single sheet shaped substrate 60, made by the method described herein, weighing approximately 56.7 grams was attached to the peripheral wall 62 of a metallic can 64 using an adhesive.
  • the can 64 was capable of containing 6.5 ounces (190 ml) of fluid.
  • the can 64 and outer container 66 were taken into an inert atmosphere glove box.
  • the substrate 60 was then treated with a 50% by weight solution of KOH. Approximately 11.3 grams of solution was coated on the sheet and allowed to absorb into the sheet 60.
  • the can 64 with attached portable flameless heating apparatus 60 was placed inside the outer container 66.
  • the outer container 66 had openings 68.
  • the entire assembly was then placed in an oxygen impermeable container and removed from the inert atmosphere glove box.
  • thermocouple was placed in the middle of the inner can to monitor the temperature of the water.
  • An additional thermocouple was attached to the portable flameless heating apparatus 60 to monitor the exterior surface temperature of the heater. The temperature rise was monitored and recorded.
  • the water temperature 80 and portable flameless heating apparatus temperature 82 started at approximately 23.3 °C (74 °F).
  • the portable flameless heating apparatus temperature 82 rose rapidly reaching over 112.8 °C (235 °F) in less than two minutes.
  • the water temperature 80 rose more slowly reaching 71.1 °C (160 °F) in 3.6 minutes.
  • the water temperature 80 reached a maximum of 86.7 °C (188 °F) in 10.8 minutes and remained above 82.2 °C (180 °F) until the test was stopped at 15 minutes.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Thermal Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Combustion & Propulsion (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Cookers (AREA)
  • Thermotherapy And Cooling Therapy Devices (AREA)

Claims (13)

  1. Précurseur d'un appareil de chauffage à accumulation sans flamme portable capable d'être stocké dans une atmosphère contenant de l'oxygène et constitué d'un substrat poreux flexible obtenu en mélangeant les composants suivants :
    - un agent réducteur produisant une réaction exothermique en s'oxydant et sélectionné dans le groupe constitué de : zinc, aluminium et magnésium,
    - un promoteur pour la réduction d'oxygène comprenant du carbone, et
    - un agent liant qui est du polytétrafluoroéthylène ;
    et en donnant au mélange une forme désirée.
  2. Appareil de chauffage sans flamme portable comprenant :
    le précurseur d'un appareil de chauffage à accumulation sans flamme portable selon la revendication 1 mouillé avec une solution électrolytique alcaline ayant une concentration sélectionnée pour commander la vitesse de la réaction exothermique de l'agent réducteur, et
    un récipient entourant le substrat poreux pour isoler le substrat d'une atmosphère extérieure au récipient, le récipient ayant au moins une ouverture refermable pour permettre sélectivement à l'atmosphère ambiante d'accéder au substrat afin que l'oxygène réagisse avec le substrat.
  3. Appareil de chauffage sans flamme portable selon la revendication 2, dans lequel l'ouverture comprend une barrière perméable à l'oxygène.
  4. Appareil de chauffage sans flamme portable selon la revendication 2 ou 3, dans lequel l'électrolyte alcalin présent dans le substrat poreux flexible formant le précurseur de l'appareil de chauffage à accumulation sans flamme portable après mouillage est de l'hydroxyde de potassium.
  5. Précurseur de l'appareil de chauffage sans flamme portable selon la revendication 1 ou appareil de chauffage sans flamme portable selon l'une quelconque des revendications 2 à 4, dans lequel la forme désirée du substrat est un contour préformé correspondant sensiblement à un contour de la partie de la surface extérieure d'un récipient destiné à contenir un produit comestible qui est nécessaire pour le transfert de chaleur désiré de l'appareil au produit comestible.
  6. Précurseur de l'appareil de chauffage sans flamme portable selon la revendication 1, dans lequel la forme désirée du substrat est une forme de stock dimensionnée pour un reformage ou une division ultérieure en dimensions plus petites comme désiré pour une utilisation avec des applications différentes.
  7. Appareil de chauffage sans flamme portable selon l'une quelconque des revendications 2 à 5, dans lequel la forme désirée du substrat est une forme de stock dimensionnée pour un reformage ou une division ultérieure en dimensions plus petites comme désiré pour une utilisation avec des applications différentes.
  8. Appareil de chauffage sans flamme portable selon la revendication 7, dans lequel la forme de stock est sélectionnée dans le groupe constitué essentiellement d'un stock de feuilles, d'un stock de tiges, d'un stock de barres, d'un stock de tubes.
  9. Procédé de fabrication d'un appareil de chauffage sans flamme portable selon l'une quelconque des revendications 2 à 5 et 7 à 8, comprenant les étapes consistant à :
    a) mélanger un agent réducteur produisant une réaction exothermique en s'oxydant et sélectionné dans le groupe constitué de : zinc, aluminium et magnésium, un promoteur pour la réduction d'oxygène comprenant du carbone et un agent liant qui est du polytétrafluoroéthylène ; et à donner au mélange une forme désirée, fournissant ainsi le précurseur d'un appareil de chauffage sans flamme portable selon la revendication 1 ;
    b) entourer le précurseur d'un appareil de chauffage sans flamme portable d'un récipient pour isoler le substrat d'une atmosphère extérieure au récipient, le récipient ayant au moins une ouverture refermable pour permettre sélectivement à l'atmosphère ambiante d'accéder au substrat afin que l'oxygène réagisse avec le substrat,
    c) sélectionner une vitesse de réaction désirée ;
    d) sélectionner une solution électrolytique alcaline pour produire la vitesse de réaction sélectionnée ;
    e) puis stocker le substrat dans une atmosphère ambiante ou une autre atmosphère contenant de l'oxygène et ajouter la solution électrolytique sélectionnée au substrat.
  10. Procédé de fabrication d'un appareil de chauffage sans flamme portable selon la revendication 9, selon lequel la forme désirée du substrat est une forme de stock dimensionnée pour un reformage ou une division ultérieure en dimensions plus petites comme désiré pour une utilisation avec des applications différentes.
  11. Procédé selon la revendication 10, selon lequel la forme de stock est sélectionnée dans le groupe constitué essentiellement d'un stock de feuilles, d'un stock de tiges, d'un stock de barres, d'un stock de tubes.
  12. Procédé de fabrication d'un appareil de chauffage sans flamme portable selon la revendication 10 ou 11, comprenant en outre l'étape consistant à diviser le substrat de stock en forme de substrat plus petites comme désiré pour un reformage ou un conditionnement ultérieur.
  13. Procédé de fabrication d'un appareil de chauffage sans flamme portable selon la revendication 9, selon lequel la forme désirée du substrat est un contour préformé correspondant sensiblement à un contour de la partie de la surface extérieure d'un récipient destiné à contenir un produit comestible qui est nécessaire pour le transfert de chaleur désiré de l'appareil au produit comestible.
EP07800084.1A 2006-08-10 2007-08-10 Système de chauffage activé par l'oxygène et méthodes de réalisation dudit système Active EP2052183B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US83702906P 2006-08-10 2006-08-10
PCT/US2007/075740 WO2008022044A2 (fr) 2006-08-10 2007-08-10 système de chauffage activé par l'oxygène et méthodes de réalisation dudit SYSTÈME

Publications (3)

Publication Number Publication Date
EP2052183A2 EP2052183A2 (fr) 2009-04-29
EP2052183A4 EP2052183A4 (fr) 2013-01-09
EP2052183B1 true EP2052183B1 (fr) 2017-06-14

Family

ID=39083006

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07800084.1A Active EP2052183B1 (fr) 2006-08-10 2007-08-10 Système de chauffage activé par l'oxygène et méthodes de réalisation dudit système

Country Status (8)

Country Link
US (1) US20100163011A1 (fr)
EP (1) EP2052183B1 (fr)
JP (1) JP5343003B2 (fr)
CN (1) CN101523125B (fr)
AU (1) AU2007286057B2 (fr)
CA (1) CA2661282C (fr)
ES (1) ES2638492T3 (fr)
WO (1) WO2008022044A2 (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2484684A (en) * 2010-10-19 2012-04-25 Microscal Two Ltd Method of generating thermal energy
WO2013103871A1 (fr) * 2012-01-05 2013-07-11 Rechargeable Battery Corporation Dispositif de chauffage activé par oxygène, poreux
CN104780818A (zh) * 2012-10-16 2015-07-15 充电电池公司 具有电解质垫的氧活化的便携加热器
EP2908787A4 (fr) * 2012-10-19 2016-08-17 Rechargeable Battery Corp Formulations d'électrolyte pour un dispositif de chauffage portable activé par oxygène
US20140109889A1 (en) * 2012-10-19 2014-04-24 Rechargeable Battery Corporation Oxygen Activated Heater With Thermal Regulator
US20150059729A1 (en) * 2013-08-30 2015-03-05 Rechargeable Battery Corporation Package for oxygen activated portable heater
US9024360B1 (en) 2014-02-17 2015-05-05 Sonoco Development, Inc. Container having self-contained heater material
US9278796B2 (en) 2014-02-17 2016-03-08 Sonoco Development, Inc. Container having self-contained heater material
US9642736B2 (en) 2014-03-12 2017-05-09 Rechargeable Battery Corporation Thermoformable splint structure with integrally associated oxygen activated heater and method of manufacturing same
US9872795B2 (en) 2014-03-12 2018-01-23 Rechargeable Battery Corporation Thermoformable medical member with heater and method of manufacturing same
US9826878B2 (en) 2015-03-17 2017-11-28 The Clorox Company Heated cleaning articles using a reactive metal and saline heat generator
US9809789B2 (en) 2015-03-17 2017-11-07 The Clorox Company Heated cleaning articles using a calcium oxide and water heat generator
US10046325B2 (en) * 2015-03-27 2018-08-14 Rechargeable Battery Corporation Self-heating device for warming of biological samples
US20160286994A1 (en) * 2015-04-01 2016-10-06 Preston Keith Felty Disposable sleeve for a container
US9782946B2 (en) 2015-07-21 2017-10-10 Sonoco Development, Inc. Laminate structure with access openings
US11998480B2 (en) 2016-03-01 2024-06-04 The Hilsinger Company Parent, Llc Self-heating compress for moist heat delivery
USD842658S1 (en) 2017-02-08 2019-03-12 Shari Lynn Groth Insulated cup sleeve
US11865036B2 (en) 2019-09-27 2024-01-09 L'oreal Integrated heater on facial skincare mask
US10881553B1 (en) * 2019-10-03 2021-01-05 Advanced Dressing, LLC Reduced pressure device having selectively deliverable electrolyte

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0244133A2 (fr) * 1986-05-01 1987-11-04 Foseco International Limited Compositions exothermiques
US5180759A (en) * 1986-05-01 1993-01-19 Foseco International Limited Exothermic compositions
US6209457B1 (en) * 1998-08-13 2001-04-03 Technology Commercialization Corp. Method and preformed composition for controlled localized heating of a base material using an exothermic reaction

Family Cites Families (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2613664A (en) * 1950-11-03 1952-10-14 Eugene J Rivoche Self-heating container having hermetic sealing means
US3606866A (en) * 1969-05-01 1971-09-21 Gen Electric Controlled oxidation heat source
US3605720A (en) * 1970-03-16 1971-09-20 Sanders Nuclear Corp Heat source systems
US3976049A (en) * 1973-07-04 1976-08-24 Asahi Kasei Kogyo Kabushiki Kaisha Structure of warmer
US4093424A (en) * 1976-03-09 1978-06-06 Toyo Ink Manufacturing Co,, Ltd. Thermogenic compositions
JPS53142795U (fr) * 1977-04-16 1978-11-10
DE2964337D1 (en) * 1978-02-24 1983-01-27 Teijin Ltd Oxygen scavenger composition, heat-generating composition and structure, and their use as an oxygen scavenger or generator of heat
JPS5569684A (en) 1978-11-20 1980-05-26 Akinobu Fujiwara Pyrogen
JPS5835706B2 (ja) * 1979-04-19 1983-08-04 株式会社 ケミツク 使用時に水を添加して発熱させる化学かいろ
US4268272A (en) * 1979-05-22 1981-05-19 Eiichi Ito Exothermic composition and warming bag containing the same
JPS5892752A (ja) * 1981-11-28 1983-06-02 Nippon Paionikusu Kk 発熱体
CA1200540A (fr) * 1983-10-24 1986-02-11 Atomic Energy Of Canada Limited - Energie Atomique Du Canada, Limitee Methode de fabrication d'un catalyseur au silice cristallin et au platine
US4756299A (en) * 1986-12-15 1988-07-12 Hypertherm Technologies, Inc. Chemical heating pad with differing air-admitting perforation sets for different heat-generation levels
JPH0720551B2 (ja) * 1987-06-15 1995-03-08 日本電池株式会社 酸素吸脱着体
DE3867989D1 (de) * 1987-09-24 1992-03-05 Murakashi Lime Ind Mittel zur verhinderung von staubbildung.
CA1323717C (fr) * 1987-10-21 1993-10-26 Takashi Ota Revetement conducteur exothermique
US5233981A (en) * 1987-12-07 1993-08-10 Ferric Inc. Hot compress structure
US4901472A (en) * 1988-09-16 1990-02-20 Donohue Thomas P Method and apparatus for the protection of citrus trees from frost damage
US5025777A (en) * 1989-11-09 1991-06-25 Karen Worchell Chemically heated blanket
US5534021A (en) * 1994-09-01 1996-07-09 Dvoretzky; Israel Heating pad for providing heat therapy
JP4547046B2 (ja) 1995-06-29 2010-09-22 ワイス・エルエルシー ヒートセル
US6245347B1 (en) * 1995-07-28 2001-06-12 Zars, Inc. Methods and apparatus for improved administration of pharmaceutically active compounds
JPH09245847A (ja) * 1996-03-13 1997-09-19 Shin Kobe Electric Mach Co Ltd 蓄電池
US5984995A (en) * 1996-03-29 1999-11-16 The Procter & Gamble Company Heat cells
US5674270A (en) * 1996-06-27 1997-10-07 The Procter & Gamble Company Thermal pad having a common attachment and oxygen permeable side
CN1212814C (zh) * 1996-07-02 2005-08-03 日本巴伊欧尼克斯股份有限公司 片状发热体及其制造方法
US6020040A (en) * 1996-12-31 2000-02-01 The Procter & Gamble Company Thermal pack having a plurality of individual heat cells
JP2002512539A (ja) * 1996-12-31 2002-04-23 ザ、プロクター、エンド、ギャンブル、カンパニー 使い捨て式温熱首包装体
US5952124A (en) * 1997-07-22 1999-09-14 Kainthla; Ramesh C. Rechargeable electrochemical cell with modified manganese oxide positive electrode
EP1027747B1 (fr) * 1997-10-24 2002-09-04 Aer Energy Resources, Inc. Source d'energie non rechargeable a cellules metal-air et systeme de ventilation pour ladite source
US6231596B1 (en) * 1998-07-27 2001-05-15 Heat Max, Inc. Surgical instrument warming device
US20020020406A1 (en) * 1998-09-06 2002-02-21 Naoki Minami United exothermic medium and heating element using it
US6092519A (en) * 1999-03-11 2000-07-25 Welker Engineering Company Heated sample container case and method
US6453648B1 (en) * 1999-07-06 2002-09-24 Zars, Inc. Method for manufacturing a heat generating apparatus
US6289889B1 (en) * 1999-07-12 2001-09-18 Tda Research, Inc. Self-heating flexible package
US6336935B1 (en) * 1999-09-15 2002-01-08 The Procter & Gamble Company Disposable thermal body wrap
EP1106669B1 (fr) * 1999-12-09 2006-09-27 Mitsubishi Gas Chemical Company, Inc. Emballage absorbant l'oxygène à base de poudre de fer et procédé de sa production
JP2001212167A (ja) * 2000-01-31 2001-08-07 Japan Pionics Co Ltd 発熱袋
US6182294B1 (en) * 2000-06-20 2001-02-06 Debra Pulley Head covering with heat generating means
JP2003129041A (ja) * 2001-10-25 2003-05-08 Maikooru Kk 発熱組成物及びこれを用いた発熱体並びにこの発熱体の製造方法
JP4323155B2 (ja) * 2002-10-31 2009-09-02 マイコール株式会社 発熱体
JP2004208978A (ja) * 2002-12-27 2004-07-29 Mycoal Products Corp 発熱組成物及び発熱体
US7022945B1 (en) * 2003-02-08 2006-04-04 Stephanie Western Container and warmer for wipes and the like
US20040178384A1 (en) * 2003-03-13 2004-09-16 Kaoru Usui Heat-generating composition, heater made using heat-generating composition, and process for producing the same
US6886553B2 (en) * 2003-04-01 2005-05-03 Heatmax, Inc. Self-contained personal warming apparatus and method of warming
US7841202B2 (en) * 2003-06-26 2010-11-30 Madan Stephanie N Heat packages and methods of their use
JP2005021673A (ja) * 2003-06-30 2005-01-27 Kao Corp 加温具
US6920873B2 (en) * 2003-09-11 2005-07-26 Energy Conversion Devices, Inc. Portable heating pack
EP1695679B1 (fr) * 2003-12-16 2019-01-23 Kao Corporation Systeme de rechauffage a vapeur
US8257416B2 (en) * 2004-02-25 2012-09-04 Vanderschuit Carl R Therapeutic devices and methods for applying therapy
US7052167B2 (en) * 2004-02-25 2006-05-30 Vanderschuit Carl R Therapeutic devices and methods for applying therapy
JP2005307050A (ja) * 2004-04-22 2005-11-04 Kao Corp 成形体
US7856948B2 (en) * 2004-05-27 2010-12-28 Wyeth Llc Self-steaming compositions, articles comprising such compositions and methods of preparing such compositions
JPWO2006006658A1 (ja) * 2004-07-14 2008-05-01 マイコール株式会社 足温用発熱体及び足温用発熱体の製造方法
EP1782769A4 (fr) * 2004-07-14 2007-12-26 Mycoal Prod Corp Élément chauffant, méthode pour retenir la chaleur l'utilisant et matériau de remplissage moulé pour le chauffage
WO2006006648A1 (fr) * 2004-07-14 2006-01-19 Mycoal Products Corporation Composition exothermique, article exothermique et procédé de production d’un article exothermique
US7998183B2 (en) * 2004-07-14 2011-08-16 Mycoal Co., Ltd. Heat generating body
US20080029080A1 (en) * 2004-07-14 2008-02-07 Toshihiro Dodo Active Iron Powder And Heat Generating Body
US7438873B2 (en) * 2004-10-27 2008-10-21 Warmkraft, Inc. Animal scent lure with heating capacity
JP3109136U (ja) * 2004-12-01 2005-05-12 株式会社パル・コーポレーション 携帯用巻き付け型加熱・保温器
US7763061B2 (en) * 2004-12-23 2010-07-27 Kimberly-Clark Worldwide, Inc. Thermal coverings
US7338516B2 (en) * 2004-12-23 2008-03-04 Kimberly-Clark Worldwide, Inc. Method for applying an exothermic coating to a substrate
US7632365B1 (en) * 2005-06-06 2009-12-15 The United States Of America As Represented By The Secretary Of The Navy Pyrotechnic thermite composition
US7722782B2 (en) * 2005-07-12 2010-05-25 Rechargeable Battery Corporation Portable heating apparatus and metal fuel composite for use with same
US20070034202A1 (en) * 2005-08-10 2007-02-15 Imaginodix, Llc Self-contained warmer
US7878187B2 (en) * 2005-09-23 2011-02-01 Wyeth Llc Heat cells comprising exothermic compositions having absorbent gelling material
US7794649B2 (en) * 2005-09-23 2010-09-14 Wyeth Llc Method of making heat cells comprising exothermic compositions having absorbent gelling material
US7842365B2 (en) * 2005-10-18 2010-11-30 Riggs Jon M Resealable label flap and base material
US20080156893A1 (en) * 2006-12-27 2008-07-03 Youngtack Shim Portable heating systems and methods
US8864924B2 (en) * 2009-04-07 2014-10-21 Heatgenie, Inc. Solid-state thermite composition based heating device

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0244133A2 (fr) * 1986-05-01 1987-11-04 Foseco International Limited Compositions exothermiques
US5180759A (en) * 1986-05-01 1993-01-19 Foseco International Limited Exothermic compositions
US6209457B1 (en) * 1998-08-13 2001-04-03 Technology Commercialization Corp. Method and preformed composition for controlled localized heating of a base material using an exothermic reaction

Also Published As

Publication number Publication date
US20100163011A1 (en) 2010-07-01
CN101523125B (zh) 2012-06-20
EP2052183A4 (fr) 2013-01-09
CA2661282A1 (fr) 2008-02-21
JP5343003B2 (ja) 2013-11-13
ES2638492T3 (es) 2017-10-23
CN101523125A (zh) 2009-09-02
CA2661282C (fr) 2012-03-27
AU2007286057A1 (en) 2008-02-21
AU2007286057B2 (en) 2011-03-10
WO2008022044A2 (fr) 2008-02-21
EP2052183A2 (fr) 2009-04-29
WO2008022044A3 (fr) 2008-12-24
JP2010500131A (ja) 2010-01-07

Similar Documents

Publication Publication Date Title
EP2052183B1 (fr) Système de chauffage activé par l'oxygène et méthodes de réalisation dudit système
US9004059B2 (en) Reusable heater in a package
EP2011846A1 (fr) Appareil de chauffage des aliments
JPS60174455A (ja) 屈曲性電気化学加熱具
US7971585B2 (en) Hydrogen elimination and thermal energy generation in water-activated chemical heaters
US8205608B2 (en) Hydrogen elimination and thermal energy generation in water-activated chemical heaters
WO2007069735A1 (fr) Desactivateur d’oxygene et procede de fabrication d’un desactivateur d’oxygene
EP2800732A1 (fr) Dispositif de chauffage activé par oxygène, poreux
US20140102435A1 (en) Oxygen Activated Portable Heater With Electrolyte Pad
WO2020231895A1 (fr) Dispositif de chauffage activé par oxygène et son procédé de fabrication
EP1935437A1 (fr) Dispositif d'evaporation et procede d'evaporation
EP3655713B1 (fr) Sachet d'aliments autochauffant à réactifs distribués et procédé de fabrication
WO2014157726A1 (fr) Composition génératrice de chaleur, et chauffage corporel jetable utilisant ladite composition
CN104293309B (zh) 空气激活型食品自加热组合物及其制备方法与应用
CA2010562A1 (fr) Reservoir reversible pour matieres gazeuses et application corespondante
WO2014157725A1 (fr) Composition générant de la chaleur, et dispositif de chauffage corporel jetable l'utilisant
JP2022158547A (ja) 化学カイロ用外袋用フィルム
JPH06316207A (ja) タイヤウオーマー
JPS59540B2 (ja) 化学カイロ

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20090220

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA HR MK RS

RIN1 Information on inventor provided before grant (corrected)

Inventor name: TINKER, LAWRENCE, A.

Inventor name: PATEL, BHAVESH

Inventor name: SESOCK, CHARLES, EDWARD

Inventor name: KAINTHLA, RAMESH, C.

DAX Request for extension of the european patent (deleted)
REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602007051329

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: F23B0090000000

Ipc: A47J0036300000

A4 Supplementary search report drawn up and despatched

Effective date: 20121206

RIC1 Information provided on ipc code assigned before grant

Ipc: A47J 36/30 20060101AFI20121130BHEP

Ipc: C09K 5/18 20060101ALI20121130BHEP

Ipc: F24J 1/00 20060101ALI20121130BHEP

17Q First examination report despatched

Effective date: 20140224

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20170105

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 900196

Country of ref document: AT

Kind code of ref document: T

Effective date: 20170615

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602007051329

Country of ref document: DE

REG Reference to a national code

Ref country code: CH

Ref legal event code: NV

Representative=s name: FREI PATENTANWALTSBUERO AG, CH

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20170614

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2638492

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20171023

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170915

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20170928

Year of fee payment: 11

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 900196

Country of ref document: AT

Kind code of ref document: T

Effective date: 20170614

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170914

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20171014

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20171011

Year of fee payment: 11

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602007051329

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 20180216

Year of fee payment: 11

26N No opposition filed

Effective date: 20180315

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170810

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 12

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170810

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IE

Payment date: 20180830

Year of fee payment: 12

REG Reference to a national code

Ref country code: CH

Ref legal event code: PCAR

Free format text: NEW ADDRESS: POSTFACH, 8032 ZUERICH (CH)

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20180830

Year of fee payment: 12

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180831

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180831

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20070810

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180810

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20190918

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180811

Ref country code: CY

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20170614

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20170614

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20190831

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190810

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190831

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20220822

Year of fee payment: 16

Ref country code: DE

Payment date: 20220819

Year of fee payment: 16

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20220823

Year of fee payment: 16

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602007051329

Country of ref document: DE

Owner name: RBCE TECH, LLC, CLEVELAND, US

Free format text: FORMER OWNER: RECHARGEABLE BATTERY CORP., COLLEGE STATION, TEX., US

Ref country code: DE

Ref legal event code: R082

Ref document number: 602007051329

Country of ref document: DE

Representative=s name: DENNEMEYER & ASSOCIATES S.A., DE

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20230119 AND 20230125

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230521

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602007051329

Country of ref document: DE

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20230810

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230810